Canonical Allele Identifier: CA2250855603
Community Standard Title: NM_016239.4(MYO15A):c.8050T= (p.Tyr2684=)
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18153858T= , CM000679.2:g.18153858T= GRCh38
NC_000017.10:g.18057172T= , CM000679.1:g.18057172T= GRCh37
NC_000017.9:g.17997897T= NCBI36
NG_011634.1:g.50153T=
NG_011634.2:g.50153T=

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.8050T= MANE Select NP_057323.3:p.Tyr2684=
ENST00000647165.2:c.8050T= MANE Select ENSP00000495481.1:p.Tyr2684=
NM_016239.3:c.8050T= NP_057323.3:p.Tyr2684=
ENST00000205890.9:c.8050T= ENSP00000205890.5:p.Tyr2684=
ENST00000418233.7:c.-159T= ENSP00000408800.3:n.-159T=
ENST00000615845.4:c.8050T= ENSP00000481642.1:p.Tyr2684=
ENST00000644795.1:c.-159T= ENSP00000495720.1:n.-159T=
ENST00000646782.1:n.205T=
ENST00000651214.1:n.196T=
XM_011523921.1:c.8044T= XP_011522223.1:p.Tyr2682=
XM_017024714.2:c.7990T= XP_016880203.1:p.Tyr2664=
XM_017024715.2:c.8053T= XP_016880204.1:p.Tyr2685=
XR_001752809.1:n.324A=
XR_001752810.1:n.367A=